Qserve Clinical Services B.V
Information
Qserve CRO is your partner for medical device pre-CE clinical investigations, PMCF studies, registries, retrospective data collection, and surveys. Our benchmark combines our Qserve CRO team with field experience, regulatory intelligence, and a practical approach. The clinical consultants had former positions within CROs and medical device/IVD manufacturers dealing with a broad range of clinical data. Together with the regulatory and quality experience of the Qserve team, the clinical experts support manufacturers with top-class clinical strategies based on the data available. Our experts bring in-depth knowledge of Notified Body requirements, with many team members having previously held positions at Notified Bodies, offering valuable insights into processes, requirements, and clinical review challenges.
Qserve CRO is part of Qserve Group, a global leader in consulting for the medical device industry, providing practical solutions for market access, regulatory compliance, medical device approvals, and clinical trials to manufacturers of medical devices and in-vitro diagnostics worldwide. With over 100 experts across 7 offices in more than 10 countries, we deliver expert guidance tailored to your needs.
